Zobrazeno 1 - 3
of 3
pro vyhledávání: '"L P Kuyt"'
Autor:
H Joenje, Stander Jansen, Rachel A. Gibson, Charmaine Havenga, Neil V. Morgan, Eliane Gluckman, Alex J. Tipping, Thomas Pearson, Christopher G. Mathew, L P Kuyt, T. De Ravel
Publikováno v:
Proceedings of the National Academy of Sciences. 98:5734-5739
Fanconi anemia (FA) is a rare, genetically heterogeneous autosomal recessive disorder associated with progressive aplastic anemia, congenital abnormalities, and cancer. FA has a very high incidence in the Afrikaner population of South Africa, possibl
Autor:
C. J. van Asperen, A. S. P. M. Breed, J. O. Van Hemel, K. Madan, A. J. H. Hamers, L. P. Kuyt, J. M. de Pater, Dominique Smeets, T. W. J. Hustinx, M.H.E.C. Pieters, K. B. J. Gerssen-Schoorl
Publikováno v:
HUMAN GENETICS, 85(1), 15-20. SPRINGER
We report the result of investigations from 20 families with 72 carriers of the paracentric inversion inv(11)(q21q23) in the Netherlands. There is no increase in the rate of spontaneous abortions among carriers of the inversion or their partners. Als
Autor:
M. L. Kwee, L. P. Kuyt
Publikováno v:
Fanconi Anemia ISBN: 9783642741814
Fanconi anemia (FA), first described by Fanconi in 1927, is an autosomal recessive disease characterized by aplastic anemia (pancytopenia with bone marrow hypoplasia) and associated with a variety of congenital anomalies, increased risk of malignancy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::86ff5a43bc199a9fbc8fe63ad6d2fc3a
https://doi.org/10.1007/978-3-642-74179-1_2
https://doi.org/10.1007/978-3-642-74179-1_2